Tag | Content |
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EnhancerAtlas ID | HS101-25092 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:158345000-158346120 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr2:158345193-158345203 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr2:158345193-158345203 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr2:158345193-158345203 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr2:158345193-158345203 | AACAGCTGTT | - | 6.02 | TEAD1 | MA0090.2 | chr2:158345930-158345940 | ATGGAATGTG | - | 6.02 | ZNF263 | MA0528.1 | chr2:158345542-158345563 | GGAGGAAGAGGAGGAGGAGGA | + | 9.83 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_18290 | chr2:158342098-158345576 | CD4p_CD25-_Il17-_PMAstim_Th | SE_56058 | chr2:158341887-158347427 | u87 | SE_58338 | chr2:158259858-158366019 | Ly1 | SE_67887 | chr2:158341887-158347427 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I157485 | chr2 | 158342129 | 158346019 |
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Enhancer Sequence | CAGAACTCCG TTATTTGCCA TCATCAAATA TAAAGAAAAT AATGAGGAAA GAAATCATAG 60 CAGTGGAAAA TTGTACTCAT AAAAGAAATC TGACTTGTCT TATGGGTTCC TACTAACAGA 120 ACTATGTAAC ATTTTGTTGC CCGTTACTAG CCAAGGTTTT GTATTATGTA TATGGGCCAC 180 ATAAAACTGA AAAAACAGCT GTTTCCACAC ATACCCCCGT TTGCCTATAT GACACTTCTA 240 TCTCCCCTTC AGGATCTAGC TTGATGTGTC CTCACGGATG AGTGTGTCTG TCCAATAGCT 300 ACTTCCACGG GTGGCCAAGC ATCTGCATCC CTCTAAACAC CAATCCCTGT AAGAATCATT 360 AGTATCGACC CAAGTTTCAT TTCTCCTCGG TGGCCTTAAA GAAATCTTTC CGATGTCTGC 420 TGTGTCTCTA CCTGTCCTGT AGTGCTGGAG CTGGCTGGAG AGAGGCAGTA AAGGCCGTGA 480 GGCTGCCCTG TGGGAGATAT TGACCCTGCA CAGAGCTGGG GGAGGGCACA GTGCTGGCAG 540 CTGGAGGAAG AGGAGGAGGA GGAATTTGTG TGCCACTGCA AACAATACAC AGTGCCAACA 600 AAAACACCAT CCCTTTTCCC AAGAAGTTCA AAGCACTTTG CAAACATTAA CTTATGAGCC 660 CACATAGTCA CGAAGCAATT ATTACTTTAT TACACCCTTA AGATAACCAC TGCAAGCAAA 720 GTGGCTAGAA AAAAAAGAAT GCATTCATTG TTTCATTATT CCTCAGCTAT TTATTGAATG 780 CCTACTATGT GCTGGGCACT GGAGGTGGAG GAGCTCCTAT GGGCTCTCAC ACTACTCCAT 840 GCTCTTTTGC CAACCCAGTT AGGGGCCCTA AGCACTTGGC TACACTAGCT ATTATGTTTA 900 TTTACACTTT ATTTTTGCCC AAATTGTTTA ATGGAATGTG CAATGTGCTC CATTCTTCAG 960 AATGCCTATA ATGTGCTAAG TGCTAAGCGA ACACACAAAA GAAAAACTTT TAAAGTTACC 1020 TATAAATCTC ATTACCACTT TAGGAACTGG GGAATAGCAA TTCAAAGTGC TGTCTTTTAA 1080 GGTGCCATAA ACAAGCTTTA GTGTGTGCAA TCTTTGTCTC 1120
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